Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 7
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 5
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 5
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 4
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 4
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 4
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 4
rs121913272 0.752 0.400 3 179210192 missense variant T/C;G snv 3
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 2
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 2
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs770167074 1.000 0.080 4 78826060 missense variant G/A;C snv 1.6E-05; 4.0E-06 1
rs121913357 0.742 0.320 7 140781603 stop gained C/A;G;T snv 1
rs1057519883 0.742 0.280 9 21971120 missense variant C/G;T snv 1
rs121913386 0.807 0.120 9 21971018 missense variant G/A;T snv 1
rs374711533 1.000 0.080 3 36718103 missense variant G/A snv 9.2E-05 1.6E-04 1
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 1
rs121918499 0.925 0.160 10 121520048 missense variant C/A;G snv 1
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 1
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 1
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 1
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 1